Canonical Allele Identifier: CA454537679

Gene: GLI3

Linked Data

• MyVariant Identifiers: chr7:g.42088286G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.42048687G>T , CM000669.2:g.42048687G>T	GRCh38
NC_000007.13:g.42088286G>T , CM000669.1:g.42088286G>T	GRCh37
NC_000007.12:g.42054811G>T	NCBI36
NG_008434.1:g.193333C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000395925.8:c.483C>A MANE Select	ENSP00000379258.3:p.Ala161=
ENST00000677288.1:c.306C>A	ENSP00000503986.1:p.Ala102=
ENST00000677605.1:c.483C>A	ENSP00000503743.1:p.Ala161=
ENST00000678429.1:c.483C>A	ENSP00000502957.1:p.Ala161=
ENST00000395925.7:c.483C>A	ENSP00000379258.3:p.Ala161=
ENST00000448703.5:c.483C>A	ENSP00000406135.1:p.Ala161=
ENST00000479210.1:n.460C>A
NM_000168.5:c.483C>A	NP_000159.3:p.Ala161=
XM_005249703.1:c.483C>A	XP_005249760.1:p.Ala161=
XM_005249704.2:c.483C>A	XP_005249761.1:p.Ala161=
XM_011515272.1:c.483C>A	XP_011513574.1:p.Ala161=
XM_011515273.1:c.483C>A	XP_011513575.1:p.Ala161=
XM_011515274.1:c.306C>A	XP_011513576.1:p.Ala102=
XM_011515274.2:c.306C>A	XP_011513576.1:p.Ala102=
XM_017011997.1:c.480C>A	XP_016867486.1:p.Ala160=
NM_000168.6:c.483C>A MANE Select	NP_000159.3:p.Ala161=